115282
间苯二甲醛
97%
别名:
1,3-苯二甲醛
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关于此项目
线性分子式:
C6H4-1,3-(CHO)2
化学文摘社编号:
分子量:
134.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-935-8
Beilstein/REAXYS Number:
1561038
MDL number:
Assay:
97%
InChI key
IZALUMVGBVKPJD-UHFFFAOYSA-N
InChI
1S/C8H6O2/c9-5-7-2-1-3-8(4-7)6-10/h1-6H
SMILES string
O=Cc1cccc(C=O)c1
assay
97%
mp
87-88 °C (lit.)
functional group
aldehyde
Quality Level
General description
间苯二甲醛参与碱催化的 Knoevenagel 缩合反应。
Application
间苯二甲醛用于双核钉联吡啶络合物的合成。
Packaging
玻璃瓶封装
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Johanna Andersson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(36), 11037-11046 (2010-08-04)
The binuclear ruthenium complex [μ-bidppz(phen)(4)Ru(2)](4+) has been extensively studied since the discovery of its unusual threading intercalation interaction with DNA, a binding mode with extremely slow binding and dissociation kinetics. The complex has been shown to be selective towards long
The effect of outer-sphere acidity on chemical reactivity in a synthetic heterogeneous base catalyst.
John D Bass et al.
Angewandte Chemie (International ed. in English), 42(42), 5219-5222 (2003-11-06)
商品
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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